Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58098Generated: October 25, 2026

Sodium Bicarbonate → 3-(6-(trifluoromethyl)-1H-indazol-4-yl)benzenesulfonamide

https://huagongshe.com/reaction/58098

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant4-Bromo-6-(trifluoromethyl)-1H-indazoleHCID 24729232—
Reactant3-(Aminosulphonyl)benzeneboronic acidHCID 44119323—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
Solvent1,4-DioxaneHCID 31275—
Product3-(6-(trifluoromethyl)-1H-indazol-4-yl)benzenesulfonamideHCID 8978301169.5%

Reaction Conditions

Temperature140 °C

Reaction Steps

4-Bromo-6-(trifluoromethyl)-1H-indazole (40 mg, 0.151 mmol), (3-sulfamoylphenyl)boronic acid (45.5 mg, 0.226 mmol), PdCl2(dppf) (11.04 mg, 0.015 mmol), sodium bicarbonate (323 μL, 0.604 mmol), and dioxane were mixed in a 10 mL vial to give an orange suspension. The vial was sealed and then heated to 140° C. for 20 minutes in a microwave reactor. The reaction mixture was subsequently filtered and the product was purified by preparative HPLC, eluting with a gradient of 35-70% ACN in H2O (containing 10 mM NH4HCO3). The pure fractions were lyophilized to give the title compound as a white solid (35.8 mg, 69.5%). 1H NMR (400 MHz, DMSO-d6) δ ppm 7.50 (s, 2H), 7.53 (s, 1H), 7.75-7.80 (m, 1H), 7.92-7.94 (m, 1H), 8.02 (s, 1H), 8.06 (dt, J=8.02, 1.29 Hz, 1H), 8.21 (t, J=1.64 Hz, 1H), 8.40 (s, 1H); ESI-MS m/z [M+H]+ calc'd for C14H10F3N3O2S, 342.0. found 342.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434743B2
Source datasetuspto-grants-2016_09
ORD IDord-367f38fb34bc4b4e8d6789a8dc992bd1
Source noteuspto-grants-2016_09